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OncoMatch/Clinical Trials/NCT07090148

Trial of pTVG-HP+Nivo+Targeted Ablation of Resistant Lesions in Non-Castrate RecurrentOMPC

Is NCT07090148 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including pTVG-HP DNA vaccine and Anti-PD-1 monoclonal antibody for prostate cancer patients.

Phase 1RecruitingUniversity of Wisconsin, MadisonNCT07090148Data as of May 2026

Treatment: pTVG-HP DNA vaccine · Anti-PD-1 monoclonal antibodyThe goal of this clinical trial is to learn whether an experimental vaccine called pTVG-HP ("vaccine" or "DNA vaccine"), combined with a drug called nivolumab can increase the cancer-fighting ability of a person's immune cells. The main question it aims to answer is whether the combination of medicines can get rid of metastatic tumors in participants with non-castrate, recurrent, oligometastatic prostate cancer. Participants will undergo: * Treatment with pTVG-HP * Treatment with Nivolumab * Radiation Therapy

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Extracted eligibility criteria

Cancer type

Prostate Cancer

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Must have received: radical prostatectomy

Participants must have undergone radical prostatectomy

Must have received: local therapy (surgery and any adjuvant/salvage radiation therapy)

Participants must have completed local therapy by surgery, and any adjuvant/salvage radiation therapy (if required), at least 3 months prior to entry

Cannot have received: LHRH agonist or nonsteroidal antiandrogen

Exception: Neoadjuvant/adjuvant androgen deprivation therapy with radiation or at prostatectomy is acceptable if no PSA progression and ≤24 months duration

Prior treatment with an LHRH agonist or nonsteroidal antiandrogen, except in the following circumstances: Neoadjuvant/adjuvant androgen deprivation therapy administered with radiation therapy or at the time of prostatectomy is acceptable, provided that there was no evidence of PSA progression while on treatment. In this situation, patients must not have received more than 24 months of androgen deprivation treatment. Other treatment with androgen deprivation therapy is prohibited.

Cannot have received: immunosuppressive therapy (chemotherapy or chronic corticosteroids >10 mg prednisone/day)

Participants cannot have evidence of immunosuppression or have been treated with immunosuppressive therapy, such as chemotherapy or chronic treatment dose corticosteroids (greater than the equivalent of 10 mg prednisone per day), within 3 months of the first vaccination.

Cannot have received: other potential or experimental therapies for prostate cancer

Participants previously treated with other potential or experimental therapies for prostate cancer must have discontinued these treatments and completed at least a 4 week washout prior to beginning treatment.

Lab requirements

Blood counts

normal hematologic function

Kidney function

normal renal function

Liver function

normal liver function

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • University of Wisconsin - Madison · Madison, Wisconsin

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